Pure Global

“Meditech”MICROVENT RESUSCITATOR - Taiwan Registration fbd3519e6fa75d275ed263449a567cb4

Access comprehensive regulatory information for “Meditech”MICROVENT RESUSCITATOR in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fbd3519e6fa75d275ed263449a567cb4 and manufactured by B.N.O.S. Meditech Limited. The authorized representative in Taiwan is EMSTREAM CORPORATION.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
fbd3519e6fa75d275ed263449a567cb4
Registration Details
Taiwan FDA Registration: fbd3519e6fa75d275ed263449a567cb4
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Meditech”MICROVENT RESUSCITATOR
TW: “美迪泰克”氣動力式緊急呼吸器
Risk Class 2
MD

Registration Details

fbd3519e6fa75d275ed263449a567cb4

Ministry of Health Medical Device Import No. 035322

DHA05603532205

Company Information

United Kingdom

Product Details

Details are as detailed as approved Chinese instructions

D Anesthesiology

D5925 Powered Emergency Respirator

Imported from abroad

Dates and Status

Mar 10, 2022

Mar 10, 2027